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Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxy-, commonly known as bis(4-ethylphenyl) ketone, is a yellow crystalline chemical compound. It serves as a versatile building block in the synthesis of various organic compounds, particularly in the development of pharmaceuticals, agrochemicals, and other functional materials. Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxyis valued for its ability to act as a ligand in catalytic reactions and its potential as a chiral building block in asymmetric synthesis, making it an important component in the field of organic chemistry.

2768-60-7

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2768-60-7 Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxyis used as a key intermediate in the synthesis of pharmaceuticals for its ability to form complex molecular structures that can target specific biological pathways. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for the development of drugs with fewer side effects and higher efficacy.
Used in Agrochemical Industry:
In the agrochemical sector, Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxyis utilized as a precursor in the production of pesticides and other crop protection agents. Its versatility in forming stable compounds makes it suitable for creating molecules with targeted pest control properties, thereby enhancing crop yields and quality.
Used in Organic Synthesis:
Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxyis used as a building block in organic synthesis for its ability to participate in various chemical reactions, leading to the formation of a wide range of organic compounds. Its role in catalytic reactions as a ligand allows for the development of new synthetic pathways and the creation of novel molecules with unique properties.
Used in Asymmetric Synthesis:
As a chiral building block, Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxyis employed in asymmetric synthesis to produce enantiomerically pure compounds. This is particularly important in the pharmaceutical industry, where the desired biological activity often resides in one enantiomer, while the other may be inactive or even harmful. The use of Ethanone, 1,2-bis(4-ethylphenyl)-2-hydroxy- in asymmetric synthesis helps to ensure that the final product has the desired chirality and biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 2768-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2768-60:
(6*2)+(5*7)+(4*6)+(3*8)+(2*6)+(1*0)=107
107 % 10 = 7
So 2768-60-7 is a valid CAS Registry Number.

2768-60-7Upstream product

2768-60-7Relevant academic research and scientific papers

Catalytically active lead(II)-imidazolium coordination assemblies with diversified lead(II) coordination geometries

Naga Babu, Chatla,Suresh, Paladugu,Srinivas, Katam,Sathyanarayana, Arruri,Sampath, Natarajan,Prabusankar, Ganesan

, p. 8164 - 8173 (2016)

Five Pb(ii)-imidazolium carboxylate coordination assemblies with novel structural motifs were derived from the reaction between the corresponding flexible, semi flexible or rigid imidazolium carboxylic acid ligands and lead nitrate. The imidazolium linker present in these molecules likely plays a triple role such as the counter ion to balance the metal charge, the ligand being an integral part of the final product and the catalyst facilitating carbon-carbon bond formation reaction. These lead-imidazolium coordination assemblies exhibit, variable chemical and thermal stabilities, as well as catalytic activity. These newly prepared catalysts are highly active towards benzoin condensation reactions with good functional group tolerance.

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